# Serum IL-6 and PTX3 predict severe outcome from COVID-19 in ambulatory subjects: Impact for future therapeutic decisions

**Authors:** Josh Poorbaugh, Jonathan T. Sims, Lin Zhang, Ching-Yun Chang, Richard E. Higgs, Ajay Nirula, Robert J. Benschop

PMC · DOI: 10.1371/journal.pone.0324242 · PLOS One · 2025-05-27

## TL;DR

The study finds that measuring IL-6 and PTX3 in blood can predict severe outcomes in early-stage COVID-19 patients, helping guide treatment decisions.

## Contribution

The study identifies IL-6 and PTX3 as early predictors of severe outcomes in ambulatory COVID-19 patients.

## Key findings

- Baseline serum IL-6 and PTX3 levels improve prediction of severe outcomes beyond demographic factors.
- A two-marker model with IL-6 and PTX3 achieves an AUC of ROC = 0.91 for predicting hospitalization or death.
- 51 serum proteins significantly enhance predictive accuracy when combined with demographic data.

## Abstract

SARS-CoV-2 infections lead to a wide-range of outcomes from mild or asymptomatic illness to serious complications and death. While many studies have characterized hospitalized SARS-CoV-2 patient immune responses, we were interested in whether serious complications of SARS-CoV-2 infection could be predicted early in ambulatory subjects. To that end, we used samples from SARS-CoV-2-infected individuals from the placebo arm of the BLAZE-1 clinical trial who progressed to hospitalization or death compared to individuals in the same study who did not require medical intervention and investigated whether baseline serum cytokines and chemokines could predict severe outcome. High-risk demographic factors at baseline, including age, nasal pharyngeal viral load, duration from symptom onset, and BMI provide significant predictive capacity for a hospitalization or death with an AUC of ROC = 0.77. The predictive performance of our outcome modeling increased when baseline serum protein markers were included. In fact, the one-marker model indicated that there were 51 individual proteins (including known markers of inflammation like IL-6, MCP-3, CXCL10, IL-1Ra, and PTX3) that significantly increased the AUC of ROC beyond high-risk patient demographics alone to range between 0.78 to 0.88. Moreover, a two-marker model incorporating levels of both IL-6 and PTX3 further improved the prediction over the addition of a single protein marker to an AUC of ROC = 0.91. While the analytes identified in this study have been well-documented to be altered in SARS-CoV-2 infection, this analysis demonstrates the potential value of their use in predicting hospitalization or death in ambulatory participants infected with SARS-CoV-2 and could guide early treatment decisions.

## Linked entities

- **Proteins:** IL6 (interleukin 6), PTX3 (pentraxin 3), CCL7 (C-C motif chemokine ligand 7), CXCL10 (C-X-C motif chemokine ligand 10), IL1R1 (interleukin 1 receptor type 1)
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** IL1RN (interleukin 1 receptor antagonist) [NCBI Gene 3557] {aka CRMO2, DIRA, ICIL-1RA, IL-1RN, IL-1ra, IL-1ra3}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CXCL10 (C-X-C motif chemokine ligand 10) [NCBI Gene 3627] {aka C7, IFI10, INP10, IP-10, SCYB10, crg-2}, CCL7 (C-C motif chemokine ligand 7) [NCBI Gene 6354] {aka FIC, MARC, MCP-3, MCP3, NC28, SCYA6}, PTX3 (pentraxin 3) [NCBI Gene 5806] {aka TNFAIP5, TSG-14}
- **Diseases:** COVID-19 (MESH:D000086382), infected (MESH:D007239), inflammation (MESH:D007249), death (MESH:D003643)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12111355/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12111355/full.md

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Source: https://tomesphere.com/paper/PMC12111355